Pure Global

NIDEK AutoLensmeter - Indonesia BPOM Medical Device Registration

NIDEK AutoLensmeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201813846. The device is manufactured by NIDEK CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULYA HUSADA JAYA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
NIDEK AutoLensmeter
Analysis ID: AKL 11201813846

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

NIDEK CO., LTD.

Country of Origin

Japan

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Mar 02, 2023

Expiry Date

Jun 06, 2027

Product Type

Diagnostic Eye Equipment

Lens measuring instrument.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing